Skip to content

China Children's Leukemia Group (CCLG)-AML2015 study on Pediatric acute myeloid leukemia

China Children's Leukemia Group (CCLG)-AML2015 study on Pediatric acute myeloid leukemia

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-15006816
Enrollment
Unknown
Registered
2015-07-26
Start date
2015-07-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pediatic acute myeloid leukemia

Interventions

DAH+ATRA:DAH induction+ATRA maintenance
DAE+ATRA:DAE induction+ATRA maintenance
DAH+Ara-c:DAH induction+Ara-c maintenance
DAE+Ara-c:DAE induction+Ara-c maintenance

Sponsors

Capital Medical University Beijing Children’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed of AML; 2. Patients younger than 18 years old; 3. Patients who haven't received pre-treatment, except for those who receive single IT injection or Hydroxycarbamide or small-dose Ara-c for Leukocytosis; 4. Patients who have signed the Informed Consent Form.

Exclusion criteria

Exclusion criteria: 1. Acute Promyelocytic Leukemia; 2. Junior Myelomonocytic Leukemia; 3. AML secondary to Fanconi Anemia; 4. AML secondary to Kostmann Syndrome; 5. AML secondary to Shwachman Syndrome; 6. AML secondary to other Bone Marrow Failure; 7. Patients who fail to receive systematic choemotherapy according to the protocol; 8. Patients who received any anti-tumor treatment within 2 weeks, except for those who received single IT injection or Hydroxycarbamide or small-dose Ara-c for Leukocytosis and have recovered from the adverse drug reactions; 9. Uncontrolled infection of bacteria, fungi, virus or any other pathogens (infection-related symptoms and sign progress despite proper use of antibiotics or any other treatment); 10. Patients complicated with psychiatric disease or any other diseases that could affect their safety and compliance, participation, follow-up or interpretation of results.

Design outcomes

Primary

MeasureTime frame
Remission State of Bone Marrow;Minimal Residual Disease;Three year's event free survival;

Secondary

MeasureTime frame
Side effect of chemotherapy;

Countries

China

Contacts

Public ContactZheng Huyong
zhenghuyong@vip.sina.com+86 010-59617621

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026